Canonical Allele Identifier: CA399513669

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624423-G-T
• MyVariant Identifiers: chr17:g.39780675G>T (hg19) ; chr17:g.41624423G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624423G>T , CM000679.2:g.41624423G>T	GRCh38
NC_000017.10:g.39780675G>T , CM000679.1:g.39780675G>T	GRCh37
NC_000017.9:g.37034201G>T	NCBI36
NG_008625.1:g.5208C>A
NG_009090.2:g.167290C>A , LRG_401:g.167290C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.87C>A MANE Select	ENSP00000308452.8:p.Cys29Ter
ENST00000311208.12:c.87C>A	ENSP00000308452.8:p.Cys29Ter
ENST00000463128.5:c.-312-217C>A	ENSP00000468672.1:n.-312-217C>A
ENST00000491673.1:n.153C>A
ENST00000540235.5:c.-119C>A	ENSP00000441751.2:n.-119C>A
ENST00000577817.3:c.42C>A	ENSP00000467418.1:p.Cys14Ter
NM_000422.2:c.87C>A	NP_000413.1:p.Cys29Ter
NM_000422.3:c.87C>A MANE Select	NP_000413.1:p.Cys29Ter