Canonical Allele Identifier: CA8563863

Gene: KRT17

Linked Data

• dbSNP Id: rs536792008
• ExAC: 17:39780690 C / A
• gnomAD v2: 17-39780690-C-A
• gnomAD v4: 17-41624438-C-A
• MyVariant Identifiers: chr17:g.39780690C>A (hg19) ; chr17:g.41624438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624438C>A , CM000679.2:g.41624438C>A	GRCh38
NC_000017.10:g.39780690C>A , CM000679.1:g.39780690C>A	GRCh37
NC_000017.9:g.37034216C>A	NCBI36
NG_008625.1:g.5193G>T
NG_009090.2:g.167275G>T , LRG_401:g.167275G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.72G>T MANE Select	ENSP00000308452.8:p.Ser24=
ENST00000311208.12:c.72G>T	ENSP00000308452.8:p.Ser24=
ENST00000463128.5:c.-312-232G>T	ENSP00000468672.1:n.-312-232G>T
ENST00000491673.1:n.138G>T
ENST00000540235.5:c.-134G>T	ENSP00000441751.2:n.-134G>T
ENST00000577817.3:c.27G>T	ENSP00000467418.1:p.Ser9=
NM_000422.2:c.72G>T	NP_000413.1:p.Ser24=
NM_000422.3:c.72G>T MANE Select	NP_000413.1:p.Ser24=