Canonical Allele Identifier: CA500206130

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624120-G-A
• MyVariant Identifiers: chr17:g.39780372G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624120G>A , CM000679.2:g.41624120G>A	GRCh38
NC_000017.10:g.39780372G>A , CM000679.1:g.39780372G>A	GRCh37
NC_000017.9:g.37033898G>A	NCBI36
NG_008625.1:g.5511C>T
NG_009090.2:g.167593C>T , LRG_401:g.167593C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.390C>T MANE Select	ENSP00000308452.8:p.Asp130=
ENST00000311208.12:c.390C>T	ENSP00000308452.8:p.Asp130=
ENST00000463128.5:c.-226C>T	ENSP00000468672.1:n.-226C>T
ENST00000491673.1:n.456C>T
ENST00000493253.5:n.177C>T
ENST00000540235.5:c.141C>T	ENSP00000441751.2:p.Asp47=
ENST00000577817.3:c.345C>T	ENSP00000467418.1:p.Asp115=
NM_000422.2:c.390C>T	NP_000413.1:p.Asp130=
NM_000422.3:c.390C>T MANE Select	NP_000413.1:p.Asp130=