Canonical Allele Identifier: CA8563890

Gene: KRT17

Linked Data

• dbSNP Id: rs778057944
• ExAC: 17:39780764 TGGC / T
• gnomAD v2: 17-39780764-TGGC-T
• MyVariant Identifiers: chr17:g.39780765_39780767del (hg19) ; chr17:g.41624513_41624515del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624519_41624521del , CM000679.2:g.41624519_41624521del	GRCh38
NC_000017.10:g.39780771_39780773del , CM000679.1:g.39780771_39780773del	GRCh37
NC_000017.9:g.37034297_37034299del	NCBI36
NG_008625.1:g.5116_5118del
NG_009090.2:g.167198_167200del , LRG_401:g.167198_167200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-6_-4del MANE Select	ENSP00000308452.8:n.-6_-4del
ENST00000311208.12:c.-6_-4del	ENSP00000308452.8:n.-6_-4del
ENST00000463128.5:c.-313+228_-313+230del	ENSP00000468672.1:n.-313+228_-313+230del
ENST00000491673.1:n.61_63del
ENST00000540235.5:c.-211_-209del	ENSP00000441751.2:n.-211_-209del
NM_000422.2:c.-6_-4del	NP_000413.1:n.-6_-4del
NM_000422.3:c.-6_-4del MANE Select	NP_000413.1:n.-6_-4del