Canonical Allele Identifier: CA2260099930

Gene: KRT16

Linked Data

• dbSNP Id: rs1908253120

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612698G>A , CM000679.2:g.41612698G>A	GRCh38
NC_000017.10:g.39768950G>A , CM000679.1:g.39768950G>A	GRCh37
NC_000017.9:g.37022476G>A	NCBI36
NG_008301.1:g.5130C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-10C>T MANE Select	ENSP00000301653.3:n.-10C>T
ENST00000301653.8:c.-10C>T	ENSP00000301653.3:n.-10C>T
ENST00000588319.1:n.68C>T
ENST00000590990.1:c.-10C>T	ENSP00000467105.1:n.-10C>T
ENST00000593067.1:c.-313+92C>T	ENSP00000467124.1:n.-313+92C>T
NM_005557.3:c.-10C>T	NP_005548.2:n.-10C>T
NM_005557.4:c.-10C>T MANE Select	NP_005548.2:n.-10C>T