Canonical Allele Identifier: CA2637838404

Gene: KRT16

Linked Data

• gnomAD v4: 17-41612691-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612691T>A , CM000679.2:g.41612691T>A	GRCh38
NC_000017.10:g.39768943T>A , CM000679.1:g.39768943T>A	GRCh37
NC_000017.9:g.37022469T>A	NCBI36
NG_008301.1:g.5137A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-3A>T MANE Select	ENSP00000301653.3:n.-3A>T
ENST00000301653.8:c.-3A>T	ENSP00000301653.3:n.-3A>T
ENST00000588319.1:n.75A>T
ENST00000590990.1:c.-3A>T	ENSP00000467105.1:n.-3A>T
ENST00000593067.1:c.-313+99A>T	ENSP00000467124.1:n.-313+99A>T
NM_005557.3:c.-3A>T	NP_005548.2:n.-3A>T
NM_005557.4:c.-3A>T MANE Select	NP_005548.2:n.-3A>T