Canonical Allele Identifier: CA399496401

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768813G>A (hg19) ; chr17:g.41612561G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612561G>A , CM000679.2:g.41612561G>A	GRCh38
NC_000017.10:g.39768813G>A , CM000679.1:g.39768813G>A	GRCh37
NC_000017.9:g.37022339G>A	NCBI36
NG_008301.1:g.5267C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.128C>T MANE Select	ENSP00000301653.3:p.Pro43Leu
ENST00000301653.8:c.128C>T	ENSP00000301653.3:p.Pro43Leu
ENST00000588319.1:n.205C>T
ENST00000590990.1:c.128C>T	ENSP00000467105.1:p.Pro43Leu
ENST00000593067.1:c.-313+229C>T	ENSP00000467124.1:n.-313+229C>T
NM_005557.3:c.128C>T	NP_005548.2:p.Pro43Leu
NM_005557.4:c.128C>T MANE Select	NP_005548.2:p.Pro43Leu