Canonical Allele Identifier: CA399511972

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624145-C-T
• MyVariant Identifiers: chr17:g.39780397C>T (hg19) ; chr17:g.41624145C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624145C>T , CM000679.2:g.41624145C>T	GRCh38
NC_000017.10:g.39780397C>T , CM000679.1:g.39780397C>T	GRCh37
NC_000017.9:g.37033923C>T	NCBI36
NG_008625.1:g.5486G>A
NG_009090.2:g.167568G>A , LRG_401:g.167568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.365G>A MANE Select	ENSP00000308452.8:p.Arg122Lys
ENST00000311208.12:c.365G>A	ENSP00000308452.8:p.Arg122Lys
ENST00000463128.5:c.-251G>A	ENSP00000468672.1:n.-251G>A
ENST00000491673.1:n.431G>A
ENST00000493253.5:n.152G>A
ENST00000540235.5:c.116G>A	ENSP00000441751.2:p.Arg39Lys
ENST00000577817.3:c.320G>A	ENSP00000467418.1:p.Arg107Lys
NM_000422.2:c.365G>A	NP_000413.1:p.Arg122Lys
NM_000422.3:c.365G>A MANE Select	NP_000413.1:p.Arg122Lys