Canonical Allele Identifier: CA2260099583

Gene: KRT16

Linked Data

• dbSNP Id: rs1597685939

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612099T>C , CM000679.2:g.41612099T>C	GRCh38
NC_000017.10:g.39768351T>C , CM000679.1:g.39768351T>C	GRCh37
NC_000017.9:g.37021877T>C	NCBI36
NG_008301.1:g.5729A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.531+59A>G MANE Select	ENSP00000301653.3:n.531+59A>G
ENST00000301653.8:c.531+59A>G	ENSP00000301653.3:n.531+59A>G
ENST00000588319.1:n.667A>G
ENST00000593067.1:c.-184+59A>G	ENSP00000467124.1:n.-184+59A>G
NM_005557.3:c.531+59A>G	NP_005548.2:n.531+59A>G
NM_005557.4:c.531+59A>G MANE Select	NP_005548.2:n.531+59A>G