Canonical Allele Identifier: CA2259745900

Gene: KRT12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866965_40866966delinsTC , CM000679.2:g.40866965_40866966delinsTC	GRCh38
NC_000017.10:g.39023217_39023218delinsTC , CM000679.1:g.39023217_39023218delinsTC	GRCh37
NC_000017.9:g.36276743_36276744delinsTC	NCBI36
NG_008077.1:g.5245_5246delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.221_222delinsGA MANE Select	ENSP00000251643.4:p.Gly74=
ENST00000647902.1:c.211+10_211+11delinsGA	ENSP00000497770.1:n.211+10_211+11delinsGA
ENST00000251643.4:c.221_222delinsGA	ENSP00000251643.4:p.Gly74=
NM_000223.3:c.221_222delinsGA	NP_000214.1:p.Gly74=
XR_934754.1:n.1500+16105_1500+16106delinsTC
XR_934754.2:n.2008+16105_2008+16106delinsTC
NM_000223.4:c.221_222delinsGA MANE Select	NP_000214.1:p.Gly74=