Canonical Allele Identifier: CA1589902883

Gene: SPINK5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131261_148131263delinsTTC , CM000667.2:g.148131261_148131263delinsTTC	GRCh38
NC_000005.9:g.147510824_147510826delinsTTC , CM000667.1:g.147510824_147510826delinsTTC	GRCh37
NC_000005.8:g.147491017_147491019delinsTTC	NCBI36
NG_009633.1:g.72290_72292delinsTTC , LRG_110:g.72290_72292delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2967_2969delinsTTC MANE Select	ENSP00000256084.7:p.Asp989=
ENST00000256084.7:c.2967_2969delinsTTC	ENSP00000256084.7:p.Asp989=
ENST00000359874.7:c.3057_3059delinsTTC	ENSP00000352936.3:p.Asp1019=
NM_001127698.1:c.3057_3059delinsTTC	NP_001121170.1:p.Asp1019=
NM_006846.3:c.2967_2969delinsTTC , LRG_110t1:c.2967_2969delinsTTC	NP_006837.2:p.Asp989=
XM_011537550.1:c.3000_3002delinsTTC	XP_011535852.1:p.Asp1000=
XM_011537551.1:c.2973_2975delinsTTC	XP_011535853.1:p.Asp991=
XM_011537551.2:c.2973_2975delinsTTC	XP_011535853.1:p.Asp991=
NM_001127698.2:c.3057_3059delinsTTC	NP_001121170.1:p.Asp1019=
NM_006846.4:c.2967_2969delinsTTC MANE Select	NP_006837.2:p.Asp989=