Canonical Allele Identifier: CA2580651430
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426032_127426033insAAGTCTCGGGAGGAGTG , CM000664.2:g.127426032_127426033insAAGTCTCGGGAGGAGTG GRCh38
NC_000002.11:g.128183608_128183609insAAGTCTCGGGAGGAGTG , CM000664.1:g.128183608_128183609insAAGTCTCGGGAGGAGTG GRCh37
NC_000002.10:g.127900078_127900079insAAGTCTCGGGAGGAGTG NCBI36
NG_016323.1:g.12613_12614insAAGTCTCGGGAGGAGTG , LRG_599:g.12613_12614insAAGTCTCGGGAGGAGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.536-53_536-52insAAGTCTCGGGAGGAGTG MANE Select ENSP00000234071.4:n.536-53_536-52insAAGTCTCGGGAGGAGTG
ENST00000234071.7:c.536-53_536-52insAAGTCTCGGGAGGAGTG ENSP00000234071.3:n.536-53_536-52insAAGTCTCGGGAGGAGTG
ENST00000402125.2:c.121-2325_121-2324insAAGTCTCGGGAGGAGTG
ENST00000409048.1:c.638-53_638-52insAAGTCTCGGGAGGAGTG ENSP00000386679.1:n.638-53_638-52insAAGTCTCGGGAGGAGTG
ENST00000442644.5:c.479-53_479-52insAAGTCTCGGGAGGAGTG ENSP00000411241.1:n.479-53_479-52insAAGTCTCGGGAGGAGTG
ENST00000464089.1:n.122-53_122-52insAAGTCTCGGGAGGAGTG
NM_000312.3:c.536-53_536-52insAAGTCTCGGGAGGAGTG , LRG_599t1:c.536-53_536-52insAAGTCTCGGGAGGAGTG NP_000303.1:n.536-53_536-52insAAGTCTCGGGAGGAGTG
XM_005263715.3:c.719-53_719-52insAAGTCTCGGGAGGAGTG XP_005263772.1:n.719-53_719-52insAAGTCTCGGGAGGAGTG
XM_005263716.3:c.701-53_701-52insAAGTCTCGGGAGGAGTG XP_005263773.1:n.701-53_701-52insAAGTCTCGGGAGGAGTG
XM_005263717.3:c.599-53_599-52insAAGTCTCGGGAGGAGTG XP_005263774.1:n.599-53_599-52insAAGTCTCGGGAGGAGTG
XM_005263717.4:c.599-53_599-52insAAGTCTCGGGAGGAGTG XP_005263774.1:n.599-53_599-52insAAGTCTCGGGAGGAGTG
XM_017004505.1:c.779-53_779-52insAAGTCTCGGGAGGAGTG XP_016859994.1:n.779-53_779-52insAAGTCTCGGGAGGAGTG
XM_024453002.1:c.881-53_881-52insAAGTCTCGGGAGGAGTG XP_024308770.1:n.881-53_881-52insAAGTCTCGGGAGGAGTG
XM_024453003.1:c.821-53_821-52insAAGTCTCGGGAGGAGTG XP_024308771.1:n.821-53_821-52insAAGTCTCGGGAGGAGTG
XM_024453004.1:c.719-53_719-52insAAGTCTCGGGAGGAGTG XP_024308772.1:n.719-53_719-52insAAGTCTCGGGAGGAGTG
XM_024453005.1:c.701-53_701-52insAAGTCTCGGGAGGAGTG XP_024308773.1:n.701-53_701-52insAAGTCTCGGGAGGAGTG
XM_024453006.1:c.638-53_638-52insAAGTCTCGGGAGGAGTG XP_024308774.1:n.638-53_638-52insAAGTCTCGGGAGGAGTG
XR_923313.2:n.4553_4554insACTCCTCCCGAGACTTC
NM_000312.4:c.536-53_536-52insAAGTCTCGGGAGGAGTG MANE Select NP_000303.1:n.536-53_536-52insAAGTCTCGGGAGGAGTG
NM_001375602.1:c.719-53_719-52insAAGTCTCGGGAGGAGTG NP_001362531.1:n.719-53_719-52insAAGTCTCGGGAGGAGTG
NM_001375603.1:c.701-53_701-52insAAGTCTCGGGAGGAGTG NP_001362532.1:n.701-53_701-52insAAGTCTCGGGAGGAGTG
NM_001375604.1:c.599-53_599-52insAAGTCTCGGGAGGAGTG NP_001362533.1:n.599-53_599-52insAAGTCTCGGGAGGAGTG
NM_001375605.1:c.638-53_638-52insAAGTCTCGGGAGGAGTG NP_001362534.1:n.638-53_638-52insAAGTCTCGGGAGGAGTG
NM_001375606.1:c.704-53_704-52insAAGTCTCGGGAGGAGTG NP_001362535.1:n.704-53_704-52insAAGTCTCGGGAGGAGTG
NM_001375607.1:c.722-53_722-52insAAGTCTCGGGAGGAGTG NP_001362536.1:n.722-53_722-52insAAGTCTCGGGAGGAGTG
NM_001375608.1:c.479-53_479-52insAAGTCTCGGGAGGAGTG NP_001362537.1:n.479-53_479-52insAAGTCTCGGGAGGAGTG
NM_001375609.1:c.512-53_512-52insAAGTCTCGGGAGGAGTG NP_001362538.1:n.512-53_512-52insAAGTCTCGGGAGGAGTG
NM_001375610.1:c.530-53_530-52insAAGTCTCGGGAGGAGTG NP_001362539.1:n.530-53_530-52insAAGTCTCGGGAGGAGTG
NM_001375611.1:c.536-53_536-52insAAGTCTCGGGAGGAGTG NP_001362540.1:n.536-53_536-52insAAGTCTCGGGAGGAGTG
NM_001375613.1:c.536-53_536-52insAAGTCTCGGGAGGAGTG NP_001362542.1:n.536-53_536-52insAAGTCTCGGGAGGAGTG