Canonical Allele Identifier: CA500206440

Gene: KRT16

Linked Data

• dbSNP Id: rs1156754610
• MyVariant Identifiers: chr17:g.39768467G>A (hg19) ; chr17:g.41612215G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612215G>A , CM000679.2:g.41612215G>A	GRCh38
NC_000017.10:g.39768467G>A , CM000679.1:g.39768467G>A	GRCh37
NC_000017.9:g.37021993G>A	NCBI36
NG_008301.1:g.5613C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.474C>T MANE Select	ENSP00000301653.3:p.Pro158=
ENST00000301653.8:c.474C>T	ENSP00000301653.3:p.Pro158=
ENST00000588319.1:n.551C>T
ENST00000593067.1:c.-241C>T	ENSP00000467124.1:n.-241C>T
NM_005557.3:c.474C>T	NP_005548.2:p.Pro158=
NM_005557.4:c.474C>T MANE Select	NP_005548.2:p.Pro158=