Canonical Allele Identifier: CA399511451

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780335T>G (hg19) ; chr17:g.41624083T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624083T>G , CM000679.2:g.41624083T>G	GRCh38
NC_000017.10:g.39780335T>G , CM000679.1:g.39780335T>G	GRCh37
NC_000017.9:g.37033861T>G	NCBI36
NG_008625.1:g.5548A>C
NG_009090.2:g.167630A>C , LRG_401:g.167630A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.427A>C MANE Select	ENSP00000308452.8:p.Asn143His
ENST00000311208.12:c.427A>C	ENSP00000308452.8:p.Asn143His
ENST00000463128.5:c.-189A>C	ENSP00000468672.1:n.-189A>C
ENST00000491673.1:n.493A>C
ENST00000493253.5:n.214A>C
ENST00000540235.5:c.178A>C	ENSP00000441751.2:p.Asn60His
ENST00000577817.3:c.382A>C	ENSP00000467418.1:p.Asn128His
NM_000422.2:c.427A>C	NP_000413.1:p.Asn143His
NM_000422.3:c.427A>C MANE Select	NP_000413.1:p.Asn143His