Canonical Allele Identifier: CA8563892

Gene: KRT17

Linked Data

• dbSNP Id: rs757710345
• ExAC: 17:39780765 GGC / G
• MyVariant Identifiers: chr17:g.39780766_39780767del (hg19) ; chr17:g.41624514_41624515del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624515_41624516del , CM000679.2:g.41624515_41624516del	GRCh38
NC_000017.10:g.39780767_39780768del , CM000679.1:g.39780767_39780768del	GRCh37
NC_000017.9:g.37034293_37034294del	NCBI36
NG_008625.1:g.5116_5117del
NG_009090.2:g.167198_167199del , LRG_401:g.167198_167199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-6_-5del MANE Select	ENSP00000308452.8:n.-6_-5del
ENST00000311208.12:c.-6_-5del	ENSP00000308452.8:n.-6_-5del
ENST00000463128.5:c.-313+228_-313+229del	ENSP00000468672.1:n.-313+228_-313+229del
ENST00000491673.1:n.61_62del
ENST00000540235.5:c.-211_-210del	ENSP00000441751.2:n.-211_-210del
NM_000422.2:c.-6_-5del	NP_000413.1:n.-6_-5del
NM_000422.3:c.-6_-5del MANE Select	NP_000413.1:n.-6_-5del