Canonical Allele Identifier: CA772024448

Gene: KRT16

Linked Data

• dbSNP Id: rs200187418
• gnomAD v4: 17-41612752-G-A
• MyVariant Identifiers: chr17:g.39769004G>A (hg19) ; chr17:g.41612752G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612752G>A , CM000679.2:g.41612752G>A	GRCh38
NC_000017.10:g.39769004G>A , CM000679.1:g.39769004G>A	GRCh37
NC_000017.9:g.37022530G>A	NCBI36
NG_008301.1:g.5076C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-64C>T MANE Select	ENSP00000301653.3:n.-64C>T
ENST00000301653.8:c.-64C>T	ENSP00000301653.3:n.-64C>T
ENST00000588319.1:n.14C>T
ENST00000590990.1:c.-36-28C>T	ENSP00000467105.1:n.-36-28C>T
ENST00000593067.1:c.-313+38C>T	ENSP00000467124.1:n.-313+38C>T
NM_005557.3:c.-64C>T	NP_005548.2:n.-64C>T
NM_005557.4:c.-64C>T MANE Select	NP_005548.2:n.-64C>T