Canonical Allele Identifier: CA1589902905
Gene: SPINK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148131306T= , CM000667.2:g.148131306T= GRCh38
NC_000005.9:g.147510869T= , CM000667.1:g.147510869T= GRCh37
NC_000005.8:g.147491062T= NCBI36
NG_009633.1:g.72335T= , LRG_110:g.72335T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256084.8:c.3012T= MANE Select ENSP00000256084.7:p.Tyr1004=
ENST00000256084.7:c.3012T= ENSP00000256084.7:p.Tyr1004=
ENST00000359874.7:c.3102T= ENSP00000352936.3:p.Tyr1034=
NM_001127698.1:c.3102T= NP_001121170.1:p.Tyr1034=
NM_006846.3:c.3012T= , LRG_110t1:c.3012T= NP_006837.2:p.Tyr1004=
XM_011537550.1:c.3045T= XP_011535852.1:p.Tyr1015=
XM_011537551.1:c.3018T= XP_011535853.1:p.Tyr1006=
XM_011537551.2:c.3018T= XP_011535853.1:p.Tyr1006=
NM_001127698.2:c.3102T= NP_001121170.1:p.Tyr1034=
NM_006846.4:c.3012T= MANE Select NP_006837.2:p.Tyr1004=