Canonical Allele Identifier: CA399512523

Gene: KRT17

Linked Data

• dbSNP Id: rs1908647839
• MyVariant Identifiers: chr17:g.39780491G>A (hg19) ; chr17:g.41624239G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624239G>A , CM000679.2:g.41624239G>A	GRCh38
NC_000017.10:g.39780491G>A , CM000679.1:g.39780491G>A	GRCh37
NC_000017.9:g.37034017G>A	NCBI36
NG_008625.1:g.5392C>T
NG_009090.2:g.167474C>T , LRG_401:g.167474C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.271C>T MANE Select	ENSP00000308452.8:p.Leu91Phe
ENST00000311208.12:c.271C>T	ENSP00000308452.8:p.Leu91Phe
ENST00000463128.5:c.-312-33C>T	ENSP00000468672.1:n.-312-33C>T
ENST00000491673.1:n.337C>T
ENST00000493253.5:n.58C>T
ENST00000540235.5:c.66C>T	ENSP00000441751.2:p.Thr22=
ENST00000577817.3:c.226C>T	ENSP00000467418.1:p.Leu76Phe
NM_000422.2:c.271C>T	NP_000413.1:p.Leu91Phe
NM_000422.3:c.271C>T MANE Select	NP_000413.1:p.Leu91Phe