Canonical Allele Identifier: CA399497712

Gene: KRT16

Linked Data

• MyVariant Identifiers: chr17:g.39768940T>G (hg19) ; chr17:g.41612688T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612688T>G , CM000679.2:g.41612688T>G	GRCh38
NC_000017.10:g.39768940T>G , CM000679.1:g.39768940T>G	GRCh37
NC_000017.9:g.37022466T>G	NCBI36
NG_008301.1:g.5140A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.1A>C MANE Select	ENSP00000301653.3:p.Met1Leu
ENST00000301653.8:c.1A>C	ENSP00000301653.3:p.Met1Leu
ENST00000588319.1:n.78A>C
ENST00000590990.1:c.1A>C	ENSP00000467105.1:p.Met1Leu
ENST00000593067.1:c.-313+102A>C	ENSP00000467124.1:n.-313+102A>C
NM_005557.3:c.1A>C	NP_005548.2:p.Met1Leu
NM_005557.4:c.1A>C MANE Select	NP_005548.2:p.Met1Leu