Canonical Allele Identifier: CA446933217

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147486668T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148107105T>C , CM000667.2:g.148107105T>C	GRCh38
NC_000005.9:g.147486668T>C , CM000667.1:g.147486668T>C	GRCh37
NC_000005.8:g.147466861T>C	NCBI36
NG_009633.1:g.48134T>C , LRG_110:g.48134T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481286.6:n.1157T>C
ENST00000256084.8:c.1548T>C MANE Select	ENSP00000256084.7:p.Pro516=
ENST00000256084.7:c.1548T>C	ENSP00000256084.7:p.Pro516=
ENST00000359874.7:c.1548T>C	ENSP00000352936.3:p.Pro516=
ENST00000398454.5:c.1548T>C	ENSP00000381472.1:p.Pro516=
ENST00000507988.5:n.1712T>C
ENST00000508733.5:c.1491T>C	ENSP00000421519.1:p.Pro497=
NM_001127698.1:c.1548T>C	NP_001121170.1:p.Pro516=
NM_001127699.1:c.1548T>C	NP_001121171.1:p.Pro516=
NM_006846.3:c.1548T>C , LRG_110t1:c.1548T>C	NP_006837.2:p.Pro516=
XM_011537550.1:c.1491T>C	XP_011535852.1:p.Pro497=
XM_011537551.1:c.1464T>C	XP_011535853.1:p.Pro488=
XM_011537551.2:c.1464T>C	XP_011535853.1:p.Pro488=
NM_001127698.2:c.1548T>C	NP_001121170.1:p.Pro516=
NM_001127699.2:c.1548T>C	NP_001121171.1:p.Pro516=
NM_006846.4:c.1548T>C MANE Select	NP_006837.2:p.Pro516=