Canonical Allele Identifier: CA1589902887
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131269T= , CM000667.2:g.148131269T= GRCh38
NC_000005.9:g.147510832T= , CM000667.1:g.147510832T= GRCh37
NC_000005.8:g.147491025T= NCBI36
NG_009633.1:g.72298T= , LRG_110:g.72298T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.2975T= MANE Select ENSP00000256084.7:p.Met992=
ENST00000256084.7:c.2975T= ENSP00000256084.7:p.Met992=
ENST00000359874.7:c.3065T= ENSP00000352936.3:p.Met1022=
NM_001127698.1:c.3065T= NP_001121170.1:p.Met1022=
NM_006846.3:c.2975T= , LRG_110t1:c.2975T= NP_006837.2:p.Met992=
XM_011537550.1:c.3008T= XP_011535852.1:p.Met1003=
XM_011537551.1:c.2981T= XP_011535853.1:p.Met994=
XM_011537551.2:c.2981T= XP_011535853.1:p.Met994=
NM_001127698.2:c.3065T= NP_001121170.1:p.Met1022=
NM_006846.4:c.2975T= MANE Select NP_006837.2:p.Met992=