Canonical Allele Identifier: CA2637840808

Gene: KRT17

Linked Data

• gnomAD v4: 17-41623937-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41623937A>G , CM000679.2:g.41623937A>G	GRCh38
NC_000017.10:g.39780189A>G , CM000679.1:g.39780189A>G	GRCh37
NC_000017.9:g.37033715A>G	NCBI36
NG_008625.1:g.5694T>C
NG_009090.2:g.167776T>C , LRG_401:g.167776T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+141T>C MANE Select	ENSP00000308452.8:n.432+141T>C
ENST00000311208.12:c.432+141T>C	ENSP00000308452.8:n.432+141T>C
ENST00000463128.5:c.-184+141T>C	ENSP00000468672.1:n.-184+141T>C
ENST00000491673.1:n.498+141T>C
ENST00000493253.5:n.219+141T>C
ENST00000540235.5:c.183+141T>C	ENSP00000441751.2:n.183+141T>C
ENST00000577817.3:c.387+141T>C	ENSP00000467418.1:n.387+141T>C
NM_000422.2:c.432+141T>C	NP_000413.1:n.432+141T>C
NM_000422.3:c.432+141T>C MANE Select	NP_000413.1:n.432+141T>C