Canonical Allele Identifier: CA383457606

Gene: SNX19

Linked Data

• gnomAD v4: 11-130880637-T-C
• MyVariant Identifiers: chr11:g.130750532T>C (hg19) ; chr11:g.130880637T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.130880637T>C , CM000673.2:g.130880637T>C	GRCh38
NC_000011.9:g.130750532T>C , CM000673.1:g.130750532T>C	GRCh37
NC_000011.8:g.130255742T>C	NCBI36
NG_053190.1:g.40852A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265909.9:c.2743A>G MANE Select	ENSP00000265909.4:p.Met915Val
ENST00000265909.8:c.2743A>G	ENSP00000265909.4:p.Met915Val
ENST00000426933.6:c.247A>G	ENSP00000413345.2:p.Met83Val
ENST00000526579.5:n.178-926A>G
ENST00000527116.5:n.505A>G
ENST00000528555.5:c.883A>G	ENSP00000435122.1:p.Met295Val
ENST00000530330.1:n.479A>G
ENST00000530356.5:c.883A>G	ENSP00000432307.1:p.Met295Val
ENST00000533318.5:n.1103A>G
ENST00000534726.5:c.463A>G	ENSP00000433699.1:p.Met155Val
NM_001301089.1:c.883A>G	NP_001288018.1:p.Met295Val
NM_014758.2:c.2743A>G	NP_055573.2:p.Met915Val
XM_005271546.3:c.2574-926A>G	XP_005271603.1:n.2574-926A>G
XM_011542819.1:c.2989A>G	XP_011541121.1:p.Met997Val
XM_011542820.1:c.2977A>G	XP_011541122.1:p.Met993Val
XM_011542821.1:c.2869A>G	XP_011541123.1:p.Met957Val
XM_011542824.1:c.2107A>G	XP_011541126.1:p.Met703Val
XM_011542825.1:c.1264A>G	XP_011541127.1:p.Met422Val
XM_011542826.1:c.1129A>G	XP_011541128.1:p.Met377Val
XM_011542827.1:c.1009A>G	XP_011541129.1:p.Met337Val
NM_001347918.1:c.2623A>G	NP_001334847.1:p.Met875Val
NM_001347919.1:c.2574-926A>G	NP_001334848.1:n.2574-926A>G
NM_001347922.1:c.1072A>G	NP_001334851.1:p.Met358Val
NM_001347923.1:c.1018A>G	NP_001334852.1:p.Met340Val
NM_001347924.1:c.763A>G	NP_001334853.1:p.Met255Val
NM_001347925.1:c.709A>G	NP_001334854.1:p.Met237Val
NM_001347926.1:c.714-926A>G	NP_001334855.1:n.714-926A>G
NM_001347927.1:c.463A>G	NP_001334856.1:p.Met155Val
NR_144939.1:n.3376A>G
XM_011542820.2:c.2977A>G	XP_011541122.1:p.Met993Val
XM_011542821.3:c.2869A>G	XP_011541123.1:p.Met957Val
XM_011542824.2:c.2107A>G	XP_011541126.1:p.Met703Val
XM_011542825.2:c.1264A>G	XP_011541127.1:p.Met422Val
XM_011542826.2:c.1129A>G	XP_011541128.1:p.Met377Val
XM_024448521.1:c.2989A>G	XP_024304289.1:p.Met997Val
XR_001747870.1:n.3814A>G
XR_001747872.1:n.3160A>G
XR_001747873.1:n.3474A>G
NM_001301089.2:c.883A>G	NP_001288018.1:p.Met295Val
NM_001347918.2:c.2623A>G	NP_001334847.2:p.Met875Val
NM_001347919.2:c.2574-926A>G	NP_001334848.2:n.2574-926A>G
NM_001347920.2:c.*21139A>G	NP_001334849.2:n.*21139A>G
NM_001347922.2:c.1072A>G	NP_001334851.2:p.Met358Val
NM_001347923.2:c.1018A>G	NP_001334852.2:p.Met340Val
NM_001347924.2:c.763A>G	NP_001334853.1:p.Met255Val
NM_001347925.2:c.709A>G	NP_001334854.1:p.Met237Val
NM_001347926.2:c.714-926A>G	NP_001334855.1:n.714-926A>G
NM_001347927.2:c.463A>G	NP_001334856.1:p.Met155Val
NM_014758.3:c.2743A>G MANE Select	NP_055573.3:p.Met915Val
NR_144939.2:n.3368A>G